Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1TAPI Technology & API Services
03 1H. Lundbeck AS
01 3TRIMIPRAMINE MALEATE
01 1Denmark
02 1France
03 1Israel
01 1Active
02 2Inactive
01 1Complete
02 2Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4078
Submission : 1981-02-18
Status : Inactive
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17665
Submission : 2004-09-10
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-05-23
Pay. Date : 2013-02-21
DMF Number : 5900
Submission : 1985-04-22
Status : Active
Type : II
A Trimipramine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimipramine, including repackagers and relabelers. The FDA regulates Trimipramine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimipramine API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Trimipramine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimipramine supplier is an individual or a company that provides Trimipramine active pharmaceutical ingredient (API) or Trimipramine finished formulations upon request. The Trimipramine suppliers may include Trimipramine API manufacturers, exporters, distributors and traders.
click here to find a list of Trimipramine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trimipramine DMF (Drug Master File) is a document detailing the whole manufacturing process of Trimipramine active pharmaceutical ingredient (API) in detail. Different forms of Trimipramine DMFs exist exist since differing nations have different regulations, such as Trimipramine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trimipramine DMF submitted to regulatory agencies in the US is known as a USDMF. Trimipramine USDMF includes data on Trimipramine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trimipramine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Trimipramine suppliers with USDMF on PharmaCompass.
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